Evidence map›Paper›PMID 26979828›Full record

ArticleAutophagy2016

The presence of LC3B puncta and HMGB1 expression in malignant cells correlate with the immune infiltrate in breast cancer.

Sylvain Ladoire, David Enot, Laura Senovilla, François Ghiringhelli, Vichnou Poirier-Colame, Kariman Chaba, Michaela Semeraro, Marie Chaix, Frédérique Penault-Llorca, Laurent Arnould and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Autophagy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 79 papers.

0numbers the graph read from it
0cells of the map it votes in
79citing papers in PubMed
7.8field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

79 citing papers in PubMed, 106 citations in OpenAlex.

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  7. The danger theory of immunity revisited.Nature reviews. Immunology · 2024
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19 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 7 institutions in 2 countries.

Sylvain Ladoirea Department of Medical Oncology , Georges François Leclerc Center , Dijon , France.
David Enotd Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Campus , Villejuif , France.
Laura Senovillae Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers , Paris , France.
François Ghiringhellia Department of Medical Oncology , Georges François Leclerc Center , Dijon , France.
Vichnou Poirier-Colamec Institut National de la Santé et de la Recherche Médicale, U1015, Equipe labellisée Ligue Nationale Contre le Cancer, Institut Gustave Roussy , Villejuif , France.
Kariman Chabae Equipe 11 labellisée pas la Ligue Nationale contre le Cancer, Centre de Recherche des Cordeliers , Paris , France.
Michaela Semeraroc Institut National de la Santé et de la Recherche Médicale, U1015, Equipe labellisée Ligue Nationale Contre le Cancer, Institut Gustave Roussy , Villejuif , France.
Marie Chaixa Department of Medical Oncology , Georges François Leclerc Center , Dijon , France.
Frédérique Penault-Llorcaj Center Jean Perrin, EA 4677 Clermont-Ferrand , Clermont-Ferrand , France.
Laurent Arnouldl Department of Pathology and Tumor Biology , Georges François Leclerc Center , Dijon , France.
Marie Laure Poillotm Biostatistics and Epidemiology Unit, EA 4184, Centre Georges Francois Leclerc Dijon , France.
Patrick Arveuxm Biostatistics and Epidemiology Unit, EA 4184, Centre Georges Francois Leclerc Dijon , France.
Suzette Delalogen Department of Medical Oncology and Breast Cancer Group , Institut Gustave Roussy , Villejuif , France.
Fabrice Andren Department of Medical Oncology and Breast Cancer Group , Institut Gustave Roussy , Villejuif , France.
Laurence Zitvogelc Institut National de la Santé et de la Recherche Médicale, U1015, Equipe labellisée Ligue Nationale Contre le Cancer, Institut Gustave Roussy , Villejuif , France.
Guido Kroemerd Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Campus , Villejuif , France.
Inserm · FRInstitut Gustave Roussy · FRCentre Georges François Leclerc · FRUniversité de Bourgogne · FRDélégation Paris 5 · FRUniversité Clermont Auvergne · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several cell-intrinsic alterations have poor prognostic features in human breast cancer, as exemplified by the absence of MAP1LC3B/LC3B (microtubule-associated protein 1 light chain 3 β)-positive puncta in the cytoplasm (which indicates reduced autophagic flux) or the loss of nuclear HMGB1 expression by malignant cells. It is well established that breast cancer is under strong immunosurveillance, as reflected by the fact that scarce infiltration of the malignant lesion by CD8(+) cytotoxic T lymphocytes or comparatively dense infiltration by immunosuppressive cell types (such as FOXP3(+) regulatory T cells or CD68(+) tumor-associated macrophages), resulting in low CD8(+):FOXP3(+) or CD8(+):CD68(+) ratios, has a negative prognostic impact. Here, we reveal the surprising finding that cell-intrinsic features may influence the composition of the immune infiltrate in human breast cancer. Thus, the absence of LC3B puncta is correlated with intratumoral (but not peritumoral) infiltration by fewer CD8(+) cells and more FOXP3(+) or CD68(+) cells, resulting in a major drop in the CD8(+):FOXP3(+) or CD8(+):CD68(+) ratios. Moreover, absence of HMGB1 expression in nuclei correlated with a general drop in all immune effectors, in particular FOXP3(+) and CD68(+) cells, both within the tumor and close to it. Combined analysis of LC3B puncta and HMGB1 expression allowed for improved stratification of patients with respect to the characteristics of their immune infiltrate as well as overall and metastasis-free survival. It can be speculated that blocked autophagy in, or HMGB1 loss from, cancer cells may favor tumor progression due to their negative impact on anticancer immunosurveillance.

Indexed as

AutophagyBreast NeoplasmsFemaleForkhead Transcription FactorsHMGB1 ProteinHumansMicrotubule-Associated ProteinsT-Lymphocytes, CytotoxicForkhead Transcription FactorsFOXP3 protein, humanHMGB1 ProteinHMGB1 protein, humanMAP1LC3B protein, humanMicrotubule-Associated Proteinsautophagybreast cancerCD8histologyHMGB1LC3lymphocytesmacrophagespathologyprognosticTreg cells

Identifiers

PMID26979828
PMCPMC4854557
OpenAlexW2323024458

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.